Director, Global Clinical Physician – Late Oncology, GI

Bristol Myers Squibb

Director, Global Clinical Physician managing clinical trials and providing medical oversight for drug development at Bristol Myers Squibb. Requires extensive industry experience and strong communication skills.

Posted 5/9/2026full-timeMadison • New Jersey • 🇺🇸 United StatesLead💰 $275,630 - $333,998 per yearWebsite

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Serves as a primary source of medical accountability and oversight for clinical trials
Matrix management responsibilities across the internal and external network
Manages Phase 1 – Phase 3 studies, with demonstrated decision making capabilities
Provides medical and scientific expertise to cross-functional BMS colleagues
Conducts medical data review of trial data, including eligibility review
Holds responsibility for site interactions in partnership with the Global Clinical Scientist (GCS) for medical questions and education (including safety management guidelines)
Holds responsibility for assessment of key safety-related serious adverse events in partnership with Worldwide Patient Safety and oversees safety narratives
Collaborates with GCS and inputs into protocols, providing medical strategic oversight in protocol development (input on inclusion/exclusion and other safety-related clinical considerations)
Fulfills GCP and compliance obligations for clinical conduct and maintains all required training
In collaboration with the Global Clinical Development Lead, designs and develops clinical plans and protocols with a strong strategic focus based on knowledge of asset/drug, disease area and relevant science in order to meet regulatory and disease strategy targets
Provides oversight and medical accountability for a group of studies
Leads the analysis of benefit/risk for clinical development protocols in a matrix team environment working with GCS
Partners with GCS to support executional delivery of studies (e.g., site activation, enrollment status, as well as adjudication for protocol violations, significant, non-significant deviations etc.)
Identifies and builds relationships with principal investigators.
Maintains a strong medical/scientific reputation within the disease area. Has in-depth knowledge of etiology, natural history, diagnosis, and treatment of the disorder.

Requirements

What you’ll need

MD required (or x-US equivalent)
5 or more years of Industry experience and/or clinical trials experience is required
Ability to communicate and present information clearly in scientific and clinical settings
Subspecialty training in applicable therapeutic area desired
Expertise in the scientific method to test hypotheses, including statistical design, analysis, and interpretation
Knowledge of drug development process
Knowledge of the components needed to execute an effective clinical plan and protocols
Strong leadership skills with proven ability to lead and work effectively in a team environment.

Benefits

Comp & perks

Health Coverage: Medical, pharmacy, dental, and vision care.
Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).
Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.
Work-life benefits include: Paid Time Off US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees) Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays
Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

clinical trialsmedical data reviewsafety managementprotocol developmentbenefit/risk analysisstatistical designdata analysisdrug development processclinical plan executionadverse event assessment

Soft Skills

communicationpresentationleadershipteamworkrelationship buildingdecision makingstrategic focuscollaborationoversightmedical accountability

Certifications

MDsubspecialty training